• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS).

作者信息

Henry J C, van Amelsvoort T, Morris R G, Owen M J, Murphy D G M, Murphy K C

机构信息

Department of Psychology, Institute of Psychiatry, DeCrespigny Park, Denmark Hill, London SE58AF, UK.

出版信息

Neuropsychologia. 2002;40(5):471-8. doi: 10.1016/s0028-3932(01)00136-1.

DOI:10.1016/s0028-3932(01)00136-1
PMID:11749977
Abstract

Velo-cardio-facial syndrome (VCFS) is associated with deletions on the long arm of chromosome 22, mild intellectual disability, poor social interaction and a high prevalence of psychosis. However, to date there have been no studies investigating the neuropsychological functioning of adults with VCFS. We compared 19 adults with VCFS with 19 age, gender and IQ matched controls using a comprehensive neuropsychological battery. Compared to controls, adults with VCFS had significant impairments in visuoperceptual ability (Visual Object and Space Perception Battery), problem solving and planning (Tower of London) and abstract and social thinking (Comprehension WAIS-R). It is likely that haploinsufficiency (reduced gene dosage) of a neurodevelopmental gene or genes mapping to chromosome 22q11 underlies the cognitive deficits observed in individuals with VCFS.

摘要

相似文献

1
An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS).
Neuropsychologia. 2002;40(5):471-8. doi: 10.1016/s0028-3932(01)00136-1.
2
Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome.
Schizophr Res. 2004 Oct 1;70(2-3):223-32. doi: 10.1016/j.schres.2003.10.004.
3
Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome.
Br J Psychiatry. 2001 May;178:412-9. doi: 10.1192/bjp.178.5.412.
4
High rates of schizophrenia in adults with velo-cardio-facial syndrome.患有腭心面综合征的成年人中精神分裂症的高发病率。
Arch Gen Psychiatry. 1999 Oct;56(10):940-5. doi: 10.1001/archpsyc.56.10.940.
5
Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome.一种功能性儿茶酚-O-甲基转移酶基因多态性对腭心面综合征成年人脑解剖结构和认知功能的影响。
Psychol Med. 2008 Jan;38(1):89-100. doi: 10.1017/S0033291707000700. Epub 2007 May 10.
6
Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.心脏-颜面综合征中的基因、大脑发育与精神疾病表型
Dev Disabil Res Rev. 2008;14(1):59-68. doi: 10.1002/ddrr.9.
7
Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability?患有腭心面综合征(22q11缺失)的小学适龄儿童的神经心理学、学习及心理社会特征:非言语学习障碍的证据?
Child Neuropsychol. 1999 Dec;5(4):230-41. doi: 10.1076/0929-7049(199912)05:04;1-R;FT230.
8
Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia.腭心面综合征:理解精神分裂症遗传学和发病机制的模型。
Br J Psychiatry. 2001 Nov;179:397-402. doi: 10.1192/bjp.179.5.397.
9
Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.151例腭心面综合征患者22q11缺失的分子定义
Am J Hum Genet. 1997 Sep;61(3):620-9. doi: 10.1086/515508.
10
Annotation: velo-cardio-facial syndrome.注释:腭心面综合征。
J Child Psychol Psychiatry. 2005 Jun;46(6):563-71. doi: 10.1111/j.1469-7610.2005.00408.x.

引用本文的文献

1
Cognitive, adaptive and daily life functioning in adults with 22q11.2 deletion syndrome.22q11.2缺失综合征成年患者的认知、适应能力及日常生活功能
BJPsych Open. 2024 Nov 11;10(6):e203. doi: 10.1192/bjo.2024.745.
2
Extent of magnitude representation deficit and relationship with arithmetic skills in children with 22q11.2DS.22q11.2DS 患儿数量级表征缺陷的程度及其与算术技能的关系。
Orphanet J Rare Dis. 2024 Jul 3;19(1):250. doi: 10.1186/s13023-024-03263-1.
3
Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology.
22q11.2 缺失综合征患儿、青少年及成人的认知缺陷与精神病理学的关联
Transl Psychiatry. 2020 Feb 3;10(1):53. doi: 10.1038/s41398-020-0736-7.
4
Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome.量化 22q11.2 缺失综合征患儿的空间和时间表达分辨率。
J Neurodev Disord. 2019 Dec 20;11(1):40. doi: 10.1186/s11689-019-9301-1.
5
An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndrome.一种量化面部表情视觉编码受损的隐性可靠神经测量方法:来自 22q11.2 缺失综合征的证据。
Transl Psychiatry. 2019 Feb 4;9(1):67. doi: 10.1038/s41398-019-0411-z.
6
Neurocognitive Functioning in Patients with 22q11.2 Deletion Syndrome: A Meta-Analytic Review.22q11.2 缺失综合征患者的神经认知功能:一项荟萃分析综述。
Behav Genet. 2018 Jul;48(4):259-270. doi: 10.1007/s10519-018-9903-5. Epub 2018 Jun 19.
7
Neurodevelopmental outcome in 22q11.2 deletion syndrome and management.22q11.2 缺失综合征的神经发育结局与管理。
Am J Med Genet A. 2018 Oct;176(10):2160-2166. doi: 10.1002/ajmg.a.38709. Epub 2018 Apr 25.
8
Functional roles of p120ctn family of proteins in central neurons.p120ctn 家族蛋白在中枢神经元中的功能作用。
Semin Cell Dev Biol. 2017 Sep;69:70-82. doi: 10.1016/j.semcdb.2017.05.027. Epub 2017 Jun 9.
9
Visual memory profile in 22q11.2 microdeletion syndrome: are there differences in performance and neurobiological substrates between tasks linked to ventral and dorsal visual brain structures? A cross-sectional and longitudinal study.22q11.2微缺失综合征的视觉记忆特征:与腹侧和背侧视觉脑结构相关的任务在表现和神经生物学基础上是否存在差异?一项横断面和纵向研究。
J Neurodev Disord. 2016 Nov 10;8:41. doi: 10.1186/s11689-016-9174-5. eCollection 2016.
10
Neurodevelopmental Genomic Strategies in the Study of the Psychosis Spectrum.精神病谱系研究中的神经发育基因组策略
Nebr Symp Motiv. 2016;63:5-30. doi: 10.1007/978-3-319-30596-7_2.